Canonical Allele Identifier: CA348679415

Gene: NR4A2

Linked Data

• COSMIC: COSM4471497 ; COSM4471498
• MyVariant Identifiers: chr2:g.157182331G>C (hg19) ; chr2:g.156325819G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325819G>C , CM000664.2:g.156325819G>C	GRCh38
NC_000002.11:g.157182331G>C , CM000664.1:g.157182331G>C	GRCh37
NC_000002.10:g.156890577G>C	NCBI36
NG_011821.1:g.11957C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1518C>G	ENSP00000514865.1:p.Phe506Leu
ENST00000700229.1:c.686C>G
ENST00000700230.1:c.1262C>G	ENSP00000514867.1:n.1262C>G
ENST00000700231.1:c.1647C>G	ENSP00000514868.1:p.Phe549Leu
ENST00000339562.9:c.1722C>G MANE Select	ENSP00000344479.4:p.Phe574Leu
ENST00000675870.1:c.*233C>G	ENSP00000502739.1:n.*233C>G
ENST00000339562.8:c.1722C>G	ENSP00000344479.4:p.Phe574Leu
ENST00000409108.6:c.1618C>G	ENSP00000386993.2:p.Leu540Val
ENST00000409572.5:c.1722C>G	ENSP00000386747.1:p.Phe574Leu
ENST00000417764.5:c.*233C>G	ENSP00000415632.1:n.*233C>G
ENST00000417972.5:c.*233C>G	ENSP00000394671.1:n.*233C>G
ENST00000426264.5:c.1533C>G	ENSP00000389986.1:p.Phe511Leu
ENST00000429376.5:c.1429C>G	ENSP00000410952.1:p.Leu477Val
NM_006186.3:c.1722C>G	NP_006177.1:p.Phe574Leu
XM_005246621.2:c.1755C>G	XP_005246678.1:p.Phe585Leu
XM_005246622.2:c.1533C>G	XP_005246679.1:p.Phe511Leu
XM_005246623.1:c.1533C>G	XP_005246680.1:p.Phe511Leu
XM_006712553.2:c.1680C>G	XP_006712616.1:p.Phe560Leu
XM_011511246.1:c.1651C>G	XP_011509548.1:p.Leu551Val
NM_173173.2:c.1533C>G	NP_775265.1:p.Phe511Leu
XM_005246621.4:c.1755C>G	XP_005246678.1:p.Phe585Leu
XM_006712553.4:c.1680C>G	XP_006712616.1:p.Phe560Leu
XM_011511246.2:c.1651C>G	XP_011509548.1:p.Leu551Val
XM_017004219.2:c.1722C>G	XP_016859708.1:p.Phe574Leu
XM_017004220.2:c.1647C>G	XP_016859709.1:p.Phe549Leu
XR_001738751.2:n.1969C>G
XR_001738752.2:n.1791C>G
XR_427087.4:n.1848C>G
NM_006186.4:c.1722C>G MANE Select	NP_006177.1:p.Phe574Leu
NM_173173.3:c.1533C>G	NP_775265.1:p.Phe511Leu